# K092942: Vital Sleep

- Pathway: 510(k) (Traditional)
- Applicant: The Snore Reliever Company, LLC
- Decided: Jan 13, 2010 after 111 days
- Product code: LRK (Device, Anti-Snoring)
- Device class: 2
- Regulation: 21 CFR 872.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 2 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K111680: DR. Greensburg's Hybrid (2011), 6 descendants of its own
- K182312: Zyppah Anti-Snoring Device (2019), 3 descendants of its own
- K252531: Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2) (2026), 1 descendant of its own
- K201719: Vital Sleep (2021), 1 descendant of its own
- K261912: SnØreNegatØr (2026), 0 descendants of its own

## Indications for use
The Vital Sleep™ mandibular advancement device is intended for the treatment of nighttime snoring in adults.

Source page: https://510kreport.com/device/K092942
Methodology: https://510kreport.com/methodology